Basic Information

Drug ID DDPD00899 ...
Drug Name Remifentanil
Molecular Weight 376.4467
Molecular Formula C20H28N2O5
CAS Number 132875-61-7
SMILES CCC(=O)N(C1=CC=CC=C1)C1(CCN(CCC(=O)OC)CC1)C(=O)OC
External Links
DRUGBANK DB00899
PubChem Compound 60815
PDR 1076
Drugs.com Drugs.com Drug Page

Experimental Physicochemical Property

Property Name Property Value Unit Raw Value Raw Unit Reference
Log P 1.4 - 1.4 - DRUGBANK

Pharmacokinetic/ Toxicokinetic Property

Property Name Property Value Unit Raw Value Raw Unit Annotation Factor Reference
C Max 20.0 ng/ml ~20 ng/ml intravenous injection, IV; The Pharmacological Basis of Therapeutics
Clearance 2.4 L/h/kg 40.0 ml/min/kg normal,healthy; young; DRUGBANK
Clearance 3.0 L/h/kg 40-60 ml/min/kg normal,healthy; adults; patients; Elderly ↓ ;Hepatic cirrhosis, cirr → ;RD, renal impairment, Renal disease,including uremia → ; The Pharmacological Basis of Therapeutics
Clearance 2.2 L/h/kg 37 ml/min/kg intravenous injection, IV; human, homo sapiens; Human Intravenous Pharmacokinetic Dataset
Volume of Distribution 0.35 L/kg 350.0 ml/kg DRUGBANK
Volume of Distribution 0.45 L/kg 452±144 ml/kg Neonates; DRUGBANK
Volume of Distribution 0.22 L/kg 223±30.6 ml/kg Adolescents; DRUGBANK
Volume of Distribution 0.35 L/kg 0.3-0.4 L/kg normal,healthy; adults; patients; Elderly ↓ ;Hepatic cirrhosis, cirr → ;RD, renal impairment, Renal disease,including uremia → ; The Pharmacological Basis of Therapeutics
Volume of Distribution 0.40 L/kg 0.4 L/kg intravenous injection, IV; human, homo sapiens; Human Intravenous Pharmacokinetic Dataset
Half-life 0.18 h 1-20 min DRUGBANK
Half-life 0.23 h 0.13-0.33 h RD, renal impairment, Renal disease,including uremia → ;Hepatic cirrhosis, cirr → ; The Pharmacological Basis of Therapeutics
Half-life 0.80 h 0.8 h intravenous injection, IV; human, homo sapiens; Human Intravenous Pharmacokinetic Dataset
Eliminate Route 0 % ~0 % Urinary excretion; adults; Male, men; normal,healthy; surgery; human, homo sapiens; Unchanged drug; The Pharmacological Basis of Therapeutics
Protein Binding 70.0 % 70 % plasma proteins; DRUGBANK
Protein Binding 92.0 % 92 % adults; Male, men; normal,healthy; surgery; human, homo sapiens; The Pharmacological Basis of Therapeutics

Maximum Dosage

Property Name Property Value Unit Raw Value Raw Unit Annotation Brand Name Component Reference
Max dose for neonates 1.0 mcg/kg/dose 1 mcg/kg/dose intravenous injection, IV Ultiva remifentanil hydrochloride PDR
Max dose for neonates 1440.0 mg/kg/day 1 mg/kg/minute intravenous infusion, iv in drop Ultiva remifentanil hydrochloride PDR
Max dose for neonates 4.0 mcg/kg/dose 4 mcg/kg/dose intravenous injection, IV Ultiva remifentanil hydrochloride PDR
Max dose for infants 0.001 mg/kg/dose 1 mcg/kg/dose intravenous injection, IV Ultiva remifentanil hydrochloride PDR
Max dose for infants 1.872 mg/kg/day 1.3 mg/kg/min intravenous infusion, iv in drop Ultiva remifentanil hydrochloride PDR
Max dose for infants 0.004 mg/kg/dose 4 mcg/kg/dose intravenous injection, IV Ultiva remifentanil hydrochloride PDR
Max dose for children 0.001 mg/kg/dose 1 mcg/kg/dose intravenous injection, IV Ultiva remifentanil hydrochloride PDR
Max dose for children 1.3 mg/kg/minute 1.3 mg/kg/minute intravenous infusion, iv in drop Ultiva remifentanil hydrochloride PDR
Max dose for children 0.00125 mg/kg/dose 1.25 mcg/kg/dose intravenous injection, IV Ultiva remifentanil hydrochloride PDR
Max dose for adolescents 0.001 mg/kg/dose 1 mcg/kg/dose intravenous injection, IV Ultiva remifentanil hydrochloride PDR
Max dose for adolescents 2.88 mg/kg/day 2 mcg/kg/minute intravenous infusion, iv in drop Ultiva remifentanil hydrochloride PDR
Max dose for geriatric 1.0 mcg/kg/dose 1 mcg/kg/dose intravenous injection, IV Ultiva remifentanil hydrochloride PDR
Max dose for geriatric 2.88 mg/kg/day 2 mcg/kg/minute intravenous infusion, iv in drop Ultiva remifentanil hydrochloride PDR

Drug Property Radar Chart

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Note: Center: Q1-1.5*IQR, Edge: Q3+1.5*IQR; Q1: Quantile 1, Q3: Quantile 3, IQR: Q3-Q1